EP2464671A2 - A catalyst system and a process for the production of polyethylene - Google Patents
A catalyst system and a process for the production of polyethyleneInfo
- Publication number
- EP2464671A2 EP2464671A2 EP10743053A EP10743053A EP2464671A2 EP 2464671 A2 EP2464671 A2 EP 2464671A2 EP 10743053 A EP10743053 A EP 10743053A EP 10743053 A EP10743053 A EP 10743053A EP 2464671 A2 EP2464671 A2 EP 2464671A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- compound
- formula
- carbon atoms
- organic oxygen
- hydrocarbon radical
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000003054 catalyst Substances 0.000 title claims abstract description 81
- -1 polyethylene Polymers 0.000 title claims abstract description 66
- 238000000034 method Methods 0.000 title claims description 24
- 239000004698 Polyethylene Substances 0.000 title claims description 14
- 238000004519 manufacturing process Methods 0.000 title claims description 14
- 229920000573 polyethylene Polymers 0.000 title claims description 14
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 70
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 70
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 56
- 239000001301 oxygen Substances 0.000 claims abstract description 56
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 56
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 38
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 36
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 34
- 239000010936 titanium Substances 0.000 claims abstract description 33
- 239000004699 Ultra-high molecular weight polyethylene Substances 0.000 claims abstract description 27
- 229920000785 ultra high molecular weight polyethylene Polymers 0.000 claims abstract description 27
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 27
- 150000002681 magnesium compounds Chemical class 0.000 claims abstract description 26
- 238000006243 chemical reaction Methods 0.000 claims abstract description 25
- 150000001875 compounds Chemical class 0.000 claims abstract description 24
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 24
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims abstract description 23
- 150000003609 titanium compounds Chemical class 0.000 claims abstract description 22
- 150000003377 silicon compounds Chemical class 0.000 claims abstract description 21
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 20
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000002736 metal compounds Chemical class 0.000 claims abstract description 19
- 239000007787 solid Substances 0.000 claims abstract description 19
- 229910052751 metal Inorganic materials 0.000 claims abstract description 18
- 239000002184 metal Substances 0.000 claims abstract description 18
- VBJZVLUMGGDVMO-UHFFFAOYSA-N hafnium atom Chemical compound [Hf] VBJZVLUMGGDVMO-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000007795 chemical reaction product Substances 0.000 claims abstract description 12
- 229910052729 chemical element Inorganic materials 0.000 claims abstract description 9
- 230000000737 periodic effect Effects 0.000 claims abstract description 9
- 239000000243 solution Substances 0.000 claims description 31
- 239000011777 magnesium Substances 0.000 claims description 12
- 150000002363 hafnium compounds Chemical class 0.000 claims description 11
- 229910052749 magnesium Inorganic materials 0.000 claims description 11
- 150000003755 zirconium compounds Chemical class 0.000 claims description 9
- 239000002904 solvent Substances 0.000 claims description 5
- 238000010790 dilution Methods 0.000 claims description 4
- 239000012895 dilution Substances 0.000 claims description 4
- RVDLHGSZWAELAU-UHFFFAOYSA-N 5-tert-butylthiophene-2-carbonyl chloride Chemical group CC(C)(C)C1=CC=C(C(Cl)=O)S1 RVDLHGSZWAELAU-UHFFFAOYSA-N 0.000 claims description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract description 7
- 239000005977 Ethylene Substances 0.000 abstract description 7
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 45
- 239000002245 particle Substances 0.000 description 23
- 229920000642 polymer Polymers 0.000 description 21
- 238000006116 polymerization reaction Methods 0.000 description 20
- 239000000843 powder Substances 0.000 description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- UAIZDWNSWGTKFZ-UHFFFAOYSA-L ethylaluminum(2+);dichloride Chemical compound CC[Al](Cl)Cl UAIZDWNSWGTKFZ-UHFFFAOYSA-L 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 5
- 150000004703 alkoxides Chemical class 0.000 description 5
- 230000000052 comparative effect Effects 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 229910052736 halogen Inorganic materials 0.000 description 5
- 150000002367 halogens Chemical group 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 3
- KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 230000009286 beneficial effect Effects 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000000748 compression moulding Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 2
- 238000001125 extrusion Methods 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- 239000012299 nitrogen atmosphere Substances 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 229920000098 polyolefin Polymers 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- ODLMAHJVESYWTB-UHFFFAOYSA-N propylbenzene Chemical compound CCCC1=CC=CC=C1 ODLMAHJVESYWTB-UHFFFAOYSA-N 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229930195734 saturated hydrocarbon Natural products 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- 238000001542 size-exclusion chromatography Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- ORYGRKHDLWYTKX-UHFFFAOYSA-N trihexylalumane Chemical compound CCCCCC[Al](CCCCCC)CCCCCC ORYGRKHDLWYTKX-UHFFFAOYSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- NMVXHZSPDTXJSJ-UHFFFAOYSA-L 2-methylpropylaluminum(2+);dichloride Chemical compound CC(C)C[Al](Cl)Cl NMVXHZSPDTXJSJ-UHFFFAOYSA-L 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 229910019438 Mg(OC2H5)2 Inorganic materials 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229910003910 SiCl4 Inorganic materials 0.000 description 1
- 229910003087 TiOx Inorganic materials 0.000 description 1
- 229920010741 Ultra High Molecular Weight Polyethylene (UHMWPE) Polymers 0.000 description 1
- 229910003134 ZrOx Inorganic materials 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 239000002216 antistatic agent Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- HQMRIBYCTLBDAK-UHFFFAOYSA-M bis(2-methylpropyl)alumanylium;chloride Chemical compound CC(C)C[Al](Cl)CC(C)C HQMRIBYCTLBDAK-UHFFFAOYSA-M 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- VPCAAUUIFCAFRZ-UHFFFAOYSA-N butylalumane Chemical compound CCCC[AlH2] VPCAAUUIFCAFRZ-UHFFFAOYSA-N 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- RFUDQCRVCDXBGK-UHFFFAOYSA-L dichloro(propyl)alumane Chemical compound [Cl-].[Cl-].CCC[Al+2] RFUDQCRVCDXBGK-UHFFFAOYSA-L 0.000 description 1
- YNLAOSYQHBDIKW-UHFFFAOYSA-M diethylaluminium chloride Chemical compound CC[Al](Cl)CC YNLAOSYQHBDIKW-UHFFFAOYSA-M 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 229920006351 engineering plastic Polymers 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- JFICPAADTOQAMU-UHFFFAOYSA-L ethylaluminum(2+);dibromide Chemical compound CC[Al](Br)Br JFICPAADTOQAMU-UHFFFAOYSA-L 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000007943 implant Substances 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 210000003127 knee Anatomy 0.000 description 1
- 238000002356 laser light scattering Methods 0.000 description 1
- 229920004889 linear high-density polyethylene Polymers 0.000 description 1
- 229920000092 linear low density polyethylene Polymers 0.000 description 1
- 239000004707 linear low-density polyethylene Substances 0.000 description 1
- XDKQUSKHRIUJEO-UHFFFAOYSA-N magnesium;ethanolate Chemical compound [Mg+2].CC[O-].CC[O-] XDKQUSKHRIUJEO-UHFFFAOYSA-N 0.000 description 1
- CRGZYKWWYNQGEC-UHFFFAOYSA-N magnesium;methanolate Chemical compound [Mg+2].[O-]C.[O-]C CRGZYKWWYNQGEC-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002901 organomagnesium compounds Chemical class 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 239000002574 poison Substances 0.000 description 1
- 231100000614 poison Toxicity 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- HLLICFJUWSZHRJ-UHFFFAOYSA-N tioxidazole Chemical compound CCCOC1=CC=C2N=C(NC(=O)OC)SC2=C1 HLLICFJUWSZHRJ-UHFFFAOYSA-N 0.000 description 1
- VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 1
- LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 1
- PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 238000004260 weight control Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/06—Catalyst characterized by its size
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Definitions
- the present invention relates to a catalyst system and to a process for the production of polyethylene in the presence of this catalyst system.
- UHMWPE ultra high molecular weight polyethylene
- HDPE polyethylene
- HDPE typically has a molar mass between about 50000 and 300000 g/mol. Therefore, these linear polymers have an average molecular weight much higher than that of linear high density polyethylene.
- the polymer synthesis to obtain UHMWPE is disclosed in Journal of
- UHMWPE Due to the high molecular weight, UHMWPE displays bad flow ability when molten, it is difficult to mould it into a pellet form and the product has to be delivered in a powder form and even more important, it has also to be processed from powder. Consequently, the powder properties heavily determine the production process as well as the converting process. For example, this powder has to be stored and to be transported, and consequently the bulk density of the UHMWPE powder is very important. A higher bulk density may decrease clogging at its
- the bulk density of UHMWPE should be above 300 kg/m 3 and even more preferably above 350 kg/m 3 .
- the average particle size of the UHMWPE powder is an important characteristic.
- the average particle size (D 50 ) is preferably lower than 250 micrometers, more preferably below 200 micrometers.
- the particle size distribution commonly known as the "span", defined as (D 9 o-Dio)/D 5 o, should be low, preferably below 2, and even more preferably below 1.5.
- the shape of the polymer powder particles is translated from the shape of the catalyst particles, also known as the replica phenomenon.
- the average particle size of the polymer is proportional to the cube root of the catalyst yield, i.e. the grams of polymer produced per gram of catalyst. See for example Dall'Occo et al, in "Transition Metals and Organometallics as Catalysts for Olefin
- the catalyst must be able to produce UHMWPE with sufficiently high molar mass in an economic efficient way.
- the removal of the heat of polymerization is crucial and consequently the polymerization is carried out at increased temperatures to maximize reactor output per time and to reduce energy costs related to heat removal.
- organo aluminum compound having the formula AIR 3 in which R is a hydrocarbon radical containing 1 - 10 carbon atoms.
- Preferred metals of Group III of Mendeleev's Periodic System of Chemical Elements are aluminum and boron.
- the halogenide is Cl.
- the combination of the hydrocarbon solution comprising the organic oxygen containing magnesium compound, the organic oxygen containing titanium compound and the compound containing zirconium and/or hafnium and the specific mixture comprising the metal compound and the silicon compound results in a catalyst which provides a UHMWPE displaying a high molar mass, a high powder bulk density, a narrow span and an average particle size below 250 ⁇ m and furthermore shows a high catalyst activity.
- the compound containing zirconium and/or hafnium is selected from the group of organic oxygen containing zirconium and/or hafnium compounds.
- the metal compound from (b) having the formula MeR n X 3 - n is an aluminum compound having the formula AIR n X 3 - n in which X is a halogen and R is hydrocarbon radical containing 1 - 10 carbon atoms and 0 ⁇ n ⁇ 3.
- the molar ratio of aluminum from (b): titanium from (a) is lower than 1 :1.
- the molar ratio of titanium from 1 (a) (2) to the organic oxygen containing compound from 1 (a) (3) is in the range between 1 : 20 to 10: 1.
- organo aluminum compound having the formula AIR 3 in which R is a hydrocarbon radical containing 1 - 10 carbon atoms.
- This catalyst results in a polymer having a high powder bulk density, a narrow span and an average particle size below 250 micrometers.
- the catalyst has a high catalyst activity.
- the organic oxygen containing magnesium compound does not comprise a magnesium-carbon bond.
- Suitable organic oxygen containing magnesium compounds include for example alkoxides such as magnesium methylate, magnesium ethylate and magnesium isopropylate and alkylalkoxides, for example magnesium ethylethylate.
- the organic oxygen containing magnesium compound is a magnesium alkoxide.
- the magnesium alkoxide is magnesium ethoxide.
- Suitable organic oxygen containing titanium compounds and the zirconium or hafnium containing compounds may be represented by the general formula [MtO x (OR) 4 ⁇ x ]n in which Mt is selected from the group of titanium, zirconium and hafnium and R represents an organic radical, x ranges between 0 and 1 and n ranges between 1 and 6.
- [ZrO x (OR) 4-2 X ]n and hafnium compounds with the formula [HfO x (OR) 4 . 2x ] n include alkoxides, phenoxides, oxyalkoxides, condensed alkoxides, carboxylates and enolates.
- Suitable zirconium and hafnium containing compounds include mixed alkoxymetalchlorides with the formula (OR) y ZrCI 4-y and (OR) y HfCI 4-y wherein 1 ⁇ y ⁇ 3.
- the organic oxygen containing titanium compound is titanium alkoxide.
- the organic oxygen containing zirconium compound is zirconium alkoxide.
- the organic oxygen containing hafnium compound is hafnium alkoxide.
- Suitable alkoxides include for example Ti(OC 2 Hs) 4 , Ti(OC 3 H 7 ) 4 , Ti(OC 4 Hg) 4 , Ti(OC 8 H 17 ) 4 , Zr(OC 3 H 7 ),, Zr(OC 4 Hg) 4 , Zr(OC 8 HI 7 ) 4 , Hf(OC 3 H 7 ), , Hf(OC 4 Hg) 4 and Hf(OC 8 H 1 7 ) 4 .
- the titanium alkoxide is Ti(OC 4 Hg) 4 .
- the metal compound having the formula MeR n X 3 -D is an aluminum compound having the formula AIR n X 3 - n .
- AIR n X 3 -n include aluminum tri chloride, ethyl aluminum dibromide, ethyl aluminum dichloride, propyl aluminum dichloride, n-butyl aluminum
- dichloride isobutyl aluminum dichloride, diethyl aluminum chloride, diisobutyl aluminum chloride, triisobutyl aluminum and tri-n-hexyl aluminum.
- halogenide in the mixture of I (b) is an organo aluminum chloride and more preferably ethyl aluminum dichloride.
- organo aluminum compound of the formula AIR 3 include for example triethyl aluminum, triisobutyl aluminum, tri-n-hexyl aluminum and tri octyl aluminum.
- the hydrocarbon solution of organic oxygen containing magnesium compound and organic oxygen containing titanium, zirconium and hafnium compounds can be prepared according to procedures as disclosed for example in US 4178300 and EP-A-876318.
- the solutions are in general clear liquids. In case there are any solid particles, these can be removed via filtration prior to the use of the solution in the catalyst synthesis.
- the hydrocarbon is a C 4 -Ci2 saturated hydrocarbon.
- the hydrocarbon is a C 5 -C 7 saturated hydrocarbon.
- aluminum compounds specifically aluminum alkyl chlorides, are frequently used in the preparation of catalysts for polyolefins, it has surprisingly been found that the amount of aluminum compound in (b) should be unexpectedly low, typically below a molar ratio of aluminum from (b) to titanium from (a) of less then 1.
- the molar ratio of aluminum from (b): titanium from (a) is lower than 1 :1.
- this ratio is lower than 0.8:1 and more preferably this ratio is lower than 0.6:1.
- the molar ratio of chlorine from R m SiCl4. m : oxygen being present in the hydrocarbon solution (a) is lower than 3:1 and more preferably lower than 2:1.
- the molar ratio of magnesium: titanium is lower than 3:1.
- the molar ratio magnesium: titanium ranges between 0.2:1 and 3:1.
- the molar ratio Al from the aluminum compound in (b + c):Ti ranges between 0.05: 1 and 0.8: 1.
- the average particle size of the catalyst ranges between 3 ⁇ m and 30 ⁇ m. Preferably this average particle size ranges between 3 ⁇ m and 10 ⁇ m.
- the span of the particle size distribution is lower than 3.
- the catalyst of the present invention may be obtained by a first reaction between an organic oxygen containing magnesium compound, an organic oxygen containing titanium compound and an organic oxygen containing hafnium and/or zirconium compound, followed by dilution with a hydrocarbon solvent, resulting in a soluble complex after which a reaction between a hydrocarbon solution of said complex and the mixture comprising the metal compound having the formula MeR n X 3 - n and the silicon compound of formula R m SiCI 4- m takes place.
- the catalyst is obtained by a first reaction between a magnesium alkoxide, a titanium alkoxide and a zirconium alkoxide and/or hafnium alkoxide, followed by dilution with a hydrocarbon solvent, resulting in a soluble complex consisting of a mixed alkoxide containing magnesium, titanium and zirconium and/or hafnium and after which a reaction between a hydrocarbon solution of said complex and the mixture comprising the aluminum compound having the formula AIR n X3- n and the silicon compound of formula R m SiCI 4-m takes place.
- the mixture comprising the aluminum compound having the formula AIR n X3-n and the silicon compound of formula R m SiCl4 -m is preferably used as a solution in a hydrocarbon.
- a subsequent post treatment step in the presence of an aluminum alkyl or aluminum alkyl halogenide is possible.
- the sequence of the addition can be either adding the hydrocarbon solution containing the organic oxygen containing magnesium compound and organic oxygen containing titanium compound to the mixture comprising the aluminum compound having the formula AIR n X 3 - n and the silicon compound of formula R m SiCl 4 - m or the reversed.
- the hydrocarbon solution containing the organic oxygen containing magnesium compound and organic oxygen containing titanium compound is dosed to a stirred hydrocarbon solution comprising the aluminum compound having the formula AIR n X 3 - n and the silicon compound of formula R m SiCI 4-m .
- the temperature for this reaction can be any temperature below the boiling point of the used hydrocarbon. It is however beneficial to use temperatures below 6O 0 C, preferably below 5O 0 C. Generally the duration of the addition is preferably longer than 10 minutes and preferably longer than 30 minutes.
- the reaction of the hydrocarbon solution comprising the magnesium compound, preferably the organic oxygen containing magnesium compound, and the organic oxygen containing titanium, zirconium or hafnium compound with the mixture of the halogen containing silicon compound and the aluminum compound a solid precipitates and after the precipitation reaction the resulting mixture is heated to finish the reaction. After the reaction the precipitate is filtered and washed with a hydrocarbon. Other means of separation of the solids from the diluent and subsequent washings can also be applied, like for example multiple decantation steps. All steps should be performed in an inert atmosphere of nitrogen or another suitable inert gas.
- the post treatment with an aluminum compound can be performed either before the filtration and washing steps or after this procedure.
- An advantage of the catalyst according to the invention is that the productivity of the catalysts is high and consequently the catalyst residues in the polymer are very low.
- An additional advantage of the catalyst is that the synthesis to produce the catalyst is relatively simple and cheap based on readily available and relatively easy to handle compounds.
- R is a hydrocarbon radical containing 1 - 10 carbon atoms and 0 ⁇ n ⁇ 3 and a silicon compound of formula R m SiCI 4-m wherein 0 ⁇ m ⁇ 2 and R is a hydrocarbon radical containing 1 - 10 carbon atoms wherein the molar ratio of metal from (b): titanium from (a) is lower than 1 :1 and
- organo aluminum compound having the formula AIR 3 in which R is a hydrocarbon radical containing 1 - 10 carbon atoms.
- the catalyst is used in a process for the polymerisation of ethylene.
- the present invention is also directed to a process for the production of polyethylene characterised in that the polymerisation takes place in the presence of a catalyst system comprising
- MeR n X3 n wherein X is a halogenide, Me is a metal of Group III of
- R is a hydrocarbon radical containing 1 - 10 carbon atoms and 0 ⁇ n ⁇ 3 and a silicon compound of formula R m SiCI 4-m wherein 0 ⁇ m ⁇ 2 and R is a
- organo aluminum compound having the formula AIR 3 in which R is a hydrocarbon radical containing 1 - 10 carbon atoms.
- the compound containing zirconium and/or hafnium is preferably the compound containing zirconium and/or hafnium
- compounds is a compound selected from the group of organic oxygen containing zirconium and/or hafnium compounds.
- the metal compound is an aluminum compound having the formula AIR n X 3 - n in which X is a halogenide and R is a hydrocarbon radical containing 1 - 10 carbon atoms and 0 ⁇ n ⁇ 3.
- MeR n X 3 - n wherein X is a halogenide, Me is a metal of Group III of
- R is a hydrocarbon radical containing 1 - 10 carbon atoms and 0 ⁇ n ⁇ 3 and a silicon compound of formula R m SiCI 4 - m wherein 0 ⁇ m ⁇ 2 and R is a
- organo aluminum compound having the formula AIR 3 in which R is a hydrocarbon radical containing 1 - 10 carbon atoms.
- the metal compound from (b) is an aluminum compound having the formula AIR n X 3-H in which X is a halogenide and R is a hydrocarbon radical containing 1 - 10 carbon atoms and 0 ⁇ n ⁇ 3.
- the process results in polyethylene having the required properties and a high bulk density.
- the process is very suitable for the production of
- the process for the production of ethylene with the catalyst according to the invention is directed to the production of UHMWPE.
- the bulk density of the UHMWPE powder ranges between 350 kg/m 3 and 600 kg/m 3 and ranges preferably between 350 kg/m 3 and 550 kg/m 3
- the poured bulk density of the UHMWPE polymer powder is
- the ultra high molecular weight ethylene homo polymer and/or co polymer obtained with the catalyst according to the present invention is a powder having the following characteristics:
- the polymerization reaction may be performed in the gas phase or in bulk in the absence of an organic solvent, or carried out in liquid slurry in the presence of an organic diluent.
- the polymerization can be carried out batch wise or in a continuous mode. These reactions are performed in the absence of oxygen, water, or any other compounds that may act as a catalyst poison.
- Suitable solvents include for example alkanes and cycloalkanes such as for example propane, isobutane, pentane, hexane, heptane, n-octane, iso- octane, cyclohexane, and methylcyclohexane and alkylaromatics such as for example toluene, xylene, ethylbenzene, isopropylbenzene, ethyltoluene, n- propylbenzene and diethylbenzene.
- the polymerization temperature may range between 20 and 200°C and preferably between 20 and 120 0 C.
- the polymerization may be carried out in the presence of external donors in order to further modify the catalyst performance if this is desired.
- Suitable external donors are for example organic compounds containing hetero atoms which have at least one lone pair of electrons available for coordination to the catalyst components or aluminum alkyls.
- suitable external donors include alcohols, ethers, esters, silanes and amines.
- the polymerization can be carried out in the presence of an anti-static agent or anti fouling agent in an amount ranging between for example 1 and 500 ppm related to the total amount of reactor contents.
- the molecular mass of the polymer can be controlled by any means as known in the art, such as for example by adjustment of the polymerization temperature or by the addition of molecular weight control agents for example hydrogen or zinc alkyls. Due to the very high molecular weight of UHMWPE, it is difficult to analyze its molar mass by for instance Gel
- UHMWPE can be applied in very different areas where excellent impact strength and abrasive wear resistance are required. In medical applications UHMWPE is used in knee, shoulder and hip implants, high strength fibres made from UHMWPE can be found in ballistic cloth, fishing lines and nets and in the mining industry. UHMWPE may be used as hopper or bunker liners.
- EP 86481 A discloses a catalyst for olefin polymerisation comprising a hydrocarbon insoluble product obtained by reacting a silicon compound , a compound of a transition metal of groups IVa, Va and Vl a to form a reaction mixture and further reacting the obtained reaction mixture with a halogen containing organomagnesium compound having a magnesium- carbon bond to produce an intermediate product and contacting this intermediate product with an organoaluminium halide to form a hydrocarbon insoluble product.
- EP 86481 A does not disclose a mixture comprising a metal compound having the formula MeR n X 3-n and a silicon compound.
- EP 86481 A does not disclose the production of ultra high molecular weight polyethylene.
- US 4226964 discloses a process for polymerizing an olefin in the presence of a catalyst system combining an organoaluminum compound with a hydrocarbon insoluble solid catalytic component prepared by treating a hydrocarbon solution containing a magnesium compound, a titanium compound and a zirconium compound with an aluminum halide The titanium compound and the zirconium compound are halogen containing compounds.
- US 4226964 does not disclose a mixture comprising a metal compound having the formula MeR n Xa n and a silicon compound.
- US 4226964 does not disclose the production of ultra high molecular weight polyethylene. The invention will be elucidated by means of the following non- restrictive examples.
- the average particle size (D 5 o) of the catalyst was determined by the so called laser light scattering method in hexanes diluent, using
- Elongational Stress can be determined according to DIN 53493.
- This Elongational Stress sometimes also referred to as "Flow Value"
- Flow Value can subsequently be translated into the molecular weight as disclosed for example by J. Berzen et al. in The British Polymer Journal, Vol. 10, December 1978, pp 281 - 287.
- Catalyst particle size was 7.4 micrometers
- the polymerization was carried out in a 10 litre autoclave using 5 litre purified hexanes as a diluent. 8 mmols of tri-isobutyl aluminum were added to the 5 litre purified hexanes.
- the mixture was heated to 75°C and pressurized with ethylene. Subsequently slurry containing the predetermined amount of a catalyst according to the Example Il was dosed. The temperature was maintained at 75°C and the pressure was kept constant at 4 bar (0.4 Mpa) by feeding ethylene.
- the reaction was stopped when 1000 grams of ethylene has been supplied to the reactor. Stopping was performed by de-pressurizing and cooling down the reactor. The reactor contents were passed through a filter; the wet polymer powder was collected, subsequently dried, weighed and analyzed.
- the catalyst yield was 24.1 kilograms polyethylene per gram of catalyst.
- the catalyst activity was 3.9 kilograms polyethylene per gram of catalyst per hour per bar.
- the bulk density was 379 kg/m 3
- D 50 was 172 micrometers.
- the span was 1.1.
- the elongational stress value, indicative for the molecular weight was 0.457 MPa
- the mixture was cooled down to 120 0 C and subsequently diluted with 1480 ml of hexane. Upon addition of the hexane, the mixture cooled further down to 67°C. The mixture was kept at this temperature for 2 hours and
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- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
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Abstract
Description
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10743053.0A EP2464671B1 (en) | 2009-08-14 | 2010-08-13 | A catalyst system and a process for the production of polyethylene |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP09075364A EP2284199A1 (en) | 2009-08-14 | 2009-08-14 | A catalyst system and a process for the production of polyethylene |
| PCT/EP2010/004979 WO2011018237A2 (en) | 2009-08-14 | 2010-08-13 | A catalyst system and a process for the production of polyethylene |
| EP10743053.0A EP2464671B1 (en) | 2009-08-14 | 2010-08-13 | A catalyst system and a process for the production of polyethylene |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2464671A2 true EP2464671A2 (en) | 2012-06-20 |
| EP2464671B1 EP2464671B1 (en) | 2016-03-30 |
Family
ID=41719376
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09075364A Withdrawn EP2284199A1 (en) | 2009-08-14 | 2009-08-14 | A catalyst system and a process for the production of polyethylene |
| EP10743053.0A Not-in-force EP2464671B1 (en) | 2009-08-14 | 2010-08-13 | A catalyst system and a process for the production of polyethylene |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP09075364A Withdrawn EP2284199A1 (en) | 2009-08-14 | 2009-08-14 | A catalyst system and a process for the production of polyethylene |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US8841392B2 (en) |
| EP (2) | EP2284199A1 (en) |
| JP (1) | JP5764125B2 (en) |
| CN (1) | CN102471401B (en) |
| EA (1) | EA020797B1 (en) |
| ES (1) | ES2576055T3 (en) |
| WO (1) | WO2011018237A2 (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5670753B2 (en) * | 2008-03-14 | 2015-02-18 | サウディ ベーシック インダストリーズ コーポレイション | Catalyst system and process for producing polyethylene in the presence of this catalyst system |
| LT2697414T (en) * | 2011-04-13 | 2017-12-27 | Dsm Ip Assets B.V. | Creep-optimized uhmwpe fiber |
| EP2999810B1 (en) * | 2013-05-23 | 2018-08-29 | DSM IP Assets B.V. | Uhmwpe fiber |
| CN107001518A (en) * | 2014-10-16 | 2017-08-01 | Sabic环球技术有限责任公司 | Carbon monoxide-olefin polymeric for olefinic polymerization |
| JP6684791B2 (en) * | 2014-11-18 | 2020-04-22 | サビック グローバル テクノロジーズ ベスローテン フェンノートシャップ | Polyethylene homo- or copolymers with improved wear properties |
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-
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- 2010-08-13 EP EP10743053.0A patent/EP2464671B1/en not_active Not-in-force
- 2010-08-13 CN CN201080035954.6A patent/CN102471401B/en not_active Expired - Fee Related
- 2010-08-13 US US13/390,461 patent/US8841392B2/en not_active Expired - Fee Related
- 2010-08-13 EA EA201200289A patent/EA020797B1/en not_active IP Right Cessation
- 2010-08-13 WO PCT/EP2010/004979 patent/WO2011018237A2/en not_active Ceased
- 2010-08-13 JP JP2012524155A patent/JP5764125B2/en not_active Expired - Fee Related
- 2010-08-13 ES ES10743053.0T patent/ES2576055T3/en active Active
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Also Published As
| Publication number | Publication date |
|---|---|
| JP5764125B2 (en) | 2015-08-12 |
| EP2464671B1 (en) | 2016-03-30 |
| US20120149857A1 (en) | 2012-06-14 |
| EA201200289A1 (en) | 2012-07-30 |
| US8841392B2 (en) | 2014-09-23 |
| WO2011018237A2 (en) | 2011-02-17 |
| JP2013501830A (en) | 2013-01-17 |
| CN102471401A (en) | 2012-05-23 |
| EA020797B1 (en) | 2015-01-30 |
| WO2011018237A8 (en) | 2012-03-01 |
| CN102471401B (en) | 2014-07-30 |
| WO2011018237A3 (en) | 2011-08-18 |
| EP2284199A1 (en) | 2011-02-16 |
| ES2576055T3 (en) | 2016-07-05 |
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